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Imaging and CSF analyses effectively distinguish CJD from its mimics

Journal of neurology, neurosurgery and psychiatry, 2018-05, Vol.89 (5), p.461

2018

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Neuronal antibodies in patients with suspected or confirmed sporadic Creutzfeldt-Jakob disease

Journal of neurology, neurosurgery and psychiatry, 2015-06, Vol.86 (6), p.692-694

2015

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Cognitive decline heralds onset of symptomatic inherited prion disease

Brain (London, England : 1878), 2021-04, Vol.144 (3), p.989-998

2021

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Early neurophysiological biomarkers and spinal cord pathology in inherited prion disease

Brain (London, England : 1878), 2019-03, Vol.142 (3), p.760-770

2019

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The Medical Research Council Prion Disease Rating Scale: a new outcome measure for prion disease therapeutic trials developed and validated using systematic observational studies

Brain (London, England : 1878), 2013-04, Vol.136 (Pt 4), p.1116-1127

2013

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High-b-Value Diffusion MR Imaging and Basal Nuclei Apparent Diffusion Coefficient Measurements in Variant and Sporadic Creutzfeldt-Jakob Disease

American journal of neuroradiology : AJNR, 2010-03, Vol.31 (3), p.521-526

2010

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Iatrogenic CJD due to pituitary-derived growth hormone with genetically determined incubation times of up to 40 years

Brain (London, England : 1878), 2015-11, Vol.138 (Pt 11), p.3386-3399

2015

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Early neurophysiological biomarkers and spinal cord pathology in inherited prion disease

Brain (London, England : 1878), 2019-05, Vol.142 (5), p.e21-e21

2019

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MRI findings are often missed in the diagnosis of Creutzfeldt-Jakob disease

BMC neurology, 2012-12, Vol.12 (1), p.153-153, Article 153

2012

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Development of novel clinical examination scales for the measurement of disease severity in Creutzfeldt-Jakob disease

Journal of neurology, neurosurgery and psychiatry, 2022-04, Vol.93 (4), p.404

2022

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Neurological complications in Behçet's syndrome

Brain (London, England : 1878), 1999-11, Vol.122 ( Pt 11) (11), p.2183-2183

1999

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Quantitative EEG parameters correlate with the progression of human prion diseases

Journal of neurology, neurosurgery and psychiatry, 2016-10, Vol.87 (10), p.1061-1067

2016

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The inner ear and the neurologist

Journal of neurology, neurosurgery and psychiatry, 2007-02, Vol.78 (2), p.114-122

2007

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Visual vertigo: symptom assessment, spatial orientation and postural control

Brain (London, England : 1878), 2001-08, Vol.124 (8), p.1646-1656

2001

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Seed amplification and neurodegeneration marker trajectories in individuals at risk of prion disease

Brain (London, England : 1878), 2023-06, Vol.146 (6), p.2570-2583

2023

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Cognitive and social impairments in patients with superficial siderosis

Brain (London, England : 1878), 2005-05, Vol.128 (5), p.1082-1092

2005

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A novel prion protein variant in a patient with semantic dementia

Journal of neurology, neurosurgery and psychiatry, 2017-10, Vol.88 (10), p.890

2017

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Brain biopsy in dementia

Brain (London, England : 1878), 2005-09, Vol.128 (9), p.2016-2025

2005

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Rapid design and implementation of a virtual pain management programme due to COVID-19: a quality improvement initiative

British journal of pain, 2022-04, Vol.16 (2), p.191-202

2022

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Multiparameter MR imaging in the 6-OPRI variant of inherited prion disease

American journal of neuroradiology : AJNR, 2013-09, Vol.34 (9), p.1723-1730

2013

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The prognostic value of brain MRI in clinically isolated syndromes of the CNS: A 10-year follow-up

Brain (London, England : 1878), 1998-03, Vol.121 (3), p.495-503

1998

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Distinct neuropsychological profiles correspond to distribution of cortical thinning in inherited prion disease caused by insertional mutation

Journal of neurology, neurosurgery and psychiatry, 2012-01, Vol.83 (1), p.109-114

2012

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The role of [18F]fluoro-2-deoxyglucose-PET scanning in the diagnosis of paraneoplastic neurological disorders

Brain (London, England : 1878), 2001-11, Vol.124 (11), p.2223-2231

2001

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Development of prognostic models for survival and care status in sporadic Creutzfeldt-Jakob disease

Brain communications, 2022, Vol.4 (4), p.fcac201-fcac201

2022

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Enteral feeding is associated with longer survival in the advanced stages of prion disease

Brain communications, 2019-01, Vol.1 (1), p.fcz012-fcz012

2019

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Imaging and CSF analyses effectively distinguish CJD from its mimics

Neuronal antibodies in patients with suspected or confirmed sporadic Creutzfeldt-Jakob disease

Cognitive decline heralds onset of symptomatic inherited prion disease

Early neurophysiological biomarkers and spinal cord pathology in inherited prion disease

The Medical Research Council Prion Disease Rating Scale: a new outcome measure for prion disease therapeutic trials developed and validated using systematic observational studies

High-b-Value Diffusion MR Imaging and Basal Nuclei Apparent Diffusion Coefficient Measurements in Variant and Sporadic Creutzfeldt-Jakob Disease

Iatrogenic CJD due to pituitary-derived growth hormone with genetically determined incubation times of up to 40 years

Early neurophysiological biomarkers and spinal cord pathology in inherited prion disease

MRI findings are often missed in the diagnosis of Creutzfeldt-Jakob disease

Development of novel clinical examination scales for the measurement of disease severity in Creutzfeldt-Jakob disease

Neurological complications in Behçet's syndrome

Quantitative EEG parameters correlate with the progression of human prion diseases

The inner ear and the neurologist

Visual vertigo: symptom assessment, spatial orientation and postural control

Seed amplification and neurodegeneration marker trajectories in individuals at risk of prion disease

Cognitive and social impairments in patients with superficial siderosis

A novel prion protein variant in a patient with semantic dementia

Brain biopsy in dementia

Rapid design and implementation of a virtual pain management programme due to COVID-19: a quality improvement initiative

Multiparameter MR imaging in the 6-OPRI variant of inherited prion disease

The prognostic value of brain MRI in clinically isolated syndromes of the CNS: A 10-year follow-up

Distinct neuropsychological profiles correspond to distribution of cortical thinning in inherited prion disease caused by insertional mutation

The role of [18F]fluoro-2-deoxyglucose-PET scanning in the diagnosis of paraneoplastic neurological disorders

Development of prognostic models for survival and care status in sporadic Creutzfeldt-Jakob disease

Enteral feeding is associated with longer survival in the advanced stages of prion disease

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